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Sign in to claim this brandRestor3D
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 4001 NC Hwy 54, Suite 2160, Durham, NC, 27709
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 2 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-5148-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0032 | FDA UDI | Class II | Active |
| Kinos Axiom | 2831.0212 | FDA UDI | Class II | Unknown |
| Ossera™ AFX Instrumentation | 6744-3034-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.2140 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3458-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 4520-1002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4274-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1301 | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 1833-0106 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4266-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2050-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-M1412 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4652-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-14111100 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3848-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1505-4830 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1212 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1743-4270-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4054-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2901 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7015 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150807 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1742-3860-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4218-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2406 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2052-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4646-N | FDA UDI | Class II | Active |
| restor3d Total Talus Replacement | 6102-202 | FDA UDI | Unclassified | Active |
| Ossera™ AFX | 1740-3842-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-M1615 | FDA UDI | Class I | Active |
| Kinos Axiom | 3801-2306 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3472-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3846-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4658-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4072-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-17151007 | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723101005R | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-NSP-B0506 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-3154-N | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-002-18121234 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2905 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5242-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2401 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument Kit | 4110-S001 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-4660-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1101-010-181808 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-A4001 | FDA UDI | Class I | Active |
| restor3d Lumbar Instrumentation | 5113-B5002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4124-N | FDA UDI | Class II | Active |
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